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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1586303생성일: 2026년 10월 25일

Sucrose → HCID 57026341, 화합물

https://huagongshe.com/reaction/1586303

반응식

참여 물질

역할이름HCID투입량
반응물SucroseHCID 5988—
반응물4-MethoxybenzaldehydeHCID 31244—
반응물5-Hydroxy-2-carboethoxy-1-indanoneHCID 21218239—
용매EthanolHCID 702—
생성물HCID 57026341HCID 5702634174.3%

반응 단계

Twenty grams of bakers' yeast (Sigma Chemical Company, type II) are suspended in an aqueous solution containing 30 grams of sucrose in a conical flask, and the mixture is placed on an orbital shaker (220 rpm) at 30° C. for 30 minutes to initiate fermentation. Two grams of 5-hydroxy-2-carboethoxy-1-indanone is dissolved in 2 ml of 95% ethanol, the resulting solution is added to the fermenting yeast, and shaking is resumed. The reaction is followed by TLC (staining with anisaldehyde) to monitor the consumption of starting material and the production of product alcohol. After approximately 48 hours the reaction is judged complete, and the reaction is terminated by removing from the shaker and adding 20-30 grams of Celite. The resulting suspension is suction filtered through a pad of Celite and the clear yellow filtrate is extracted with ethyl acetate (4×200 ml). The extracts are combined, dried over MgSO4, filtered, and rotary evaporated to leave 1.5 grams of (1S,2R)-1-hydroxy-2-carboethoxy-5-hydroxyindane as a yellowish oil (>95% enantiomeric excess as judged by chiral chromatography).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05942644
출처 데이터셋uspto-grants-1999_08
ORD IDord-8c6135d33e614798aac8e1e79d2a7f8b
출처 메모uspto-grants-1999_08